Senior Director, Early Clinical Development

Job Summary

Responsibilities

• Clinical Monitoring Planning: Oversees and coordinates Sponsor oversight of CRO clinical Monitoring activities, including plan for internal communication and issue escalation with Clinical Study Lead (CSL)
• Clinical Surveillance: Documents ongoing Clinical Monitoring review of data for safety (with Clinical Safety Pharmacovigiliance) and quality at project level; Ensures global consistency of clinical Monitoring activities; Defines or contributes to department level surveillance activities across projects
• Study strategy: Interacts with leaders of each function to develop study strategy; Approves project or TA-level TM and biomarker strategy in collaboration with Translational Medicine and Clinical Pharmacology; Attends regulatory agency meetings and leads clinical strategy discussions
• Study planning and execution: Develops prospective contingency plans for management of key risks across a large project or a portfolio of projects or across the Therapeutic Area; Clearly defines priorities and high-level execution plans across projects within and outside of Daiichi Sankyo; Supports effective communication and decision-making process cross-functionally and cross-regionally at department level
• Study Outputs: Has strong understanding of statistics and study design principles applicable to primary and efficacy and safety endpoints in registrational trials to critically assess study conclusions and new study designs for early stage.
• External collaboration: Ensure continuous, effective alignment within / between CRO and vendors; For large, multiple indication project in late development, develops and leads Ad-Board with top tier KEEs for project level strategic advice; Consults with KEEs for advice on complex development or safety issues; Maintains and leads external collaborations and advisory panels at department level
• Matrix and Cross-Functional Leadership: Leverage scientific expertise and organizational influence to lead and align global cross-functional teams, fostering collaboration, accountability, and shared ownership of clinical development objectives. Build effective partnerships across functions, regions, and external stakeholders to navigate complex issues, resolve competing priorities, and advance program goals without direct supervisory authority. Additional Non-Study related activities: Routine senior management interactions; Influential relationship with top KOLs; Committee member, in-licensing and acquisitions

Qualifications

• Education Qualifications
• MD or MD/PhD with relevant clinical and industry experience required in clinical oncology required
• Postgraduate training in TA or related specialty required
• Experience Qualifications 7 or More Years relevant clinical experience required Travel Requirements Ability to travel up to 20% of the time. Domestic and International travel will be required.
• Daiichi Sankyo, Inc. is an equal opportunity/affirmative action employer. Qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected veteran status, age, or any other characteristic protected by law.
• Salary Range:
• USD$280,350.00 - USD$467,250.00
• Download Our Benefits Summary PDF
• Qualifications
• 7 or More Years relevant clinical experience required
• Experience
• Travel Requirements
• Ability to travel up to 20% of the time. Domestic and International travel will be required.